Guide Wire
- UID
- IMP/MD/2023/000011_d69bc356951cb011ba7eb177911663b8_2449073d8652b5bae3ca20690ac60049
- Device class
- Class D
- Brand name
- HI-TORQUE VERSATURN™ F Guide Wire
- License holder
- Abbott Healthcare Private Limited
- Approving authority
- CDSCO
- Product information
- HI-TORQUE™ Guide Wires are indicated to facilitate the delivery of catheter-based interventional devices during PTCA and PTA. This guide wire may be used with compatible stent devices during therapeutic procedures. The guide wire may be used to reach and cross a target lesion, provide a pathway within the vessel structure, facilitate the substitution of one diagnostic or interventional device for another, and to distinguish the vasculature. This guide wire may also be used to cross or assist in crossing de novo chronic total coronary occlusions (HI-TORQUE VERSATURN™ F Guide Wire)
Guide Wire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000011_d69bc356951cb011ba7eb177911663b8_2449073d8652b5bae3ca20690ac60049. This device is marketed under the brand name HI-TORQUE VERSATURN™ F Guide Wire. The license holder is Abbott Healthcare Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.
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